Canonical Allele Identifier: CA371657686

Gene: OTUD6B

Linked Data

• MyVariant Identifiers: chr8:g.92083376G>C (hg19) ; chr8:g.91071148G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.91071148G>C , CM000670.2:g.91071148G>C	GRCh38
NC_000008.10:g.92083376G>C , CM000670.1:g.92083376G>C	GRCh37
NC_000008.9:g.92152552G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000404789.8:c.93G>C MANE Select	ENSP00000384190.4:p.Gln31His
ENST00000285420.8:c.183G>C	ENSP00000285420.4:p.Gln61His
ENST00000404789.7:c.93G>C	ENSP00000384190.4:p.Gln31His
ENST00000522894.5:c.93G>C	ENSP00000428528.2:p.Gln31His
ENST00000524027.5:n.116G>C
ENST00000615618.1:c.-351G>C	ENSP00000481196.1:n.-351G>C
ENST00000617869.4:c.183G>C	ENSP00000483706.1:p.Gln61His
NM_001286745.1:c.-351G>C	NP_001273674.1:n.-351G>C
NM_016023.3:c.183G>C	NP_057107.3:p.Gln61His
XM_011517129.1:c.183G>C	XP_011515431.1:p.Gln61His
NM_001286745.2:c.-351G>C	NP_001273674.1:n.-351G>C
NM_016023.4:c.93G>C	NP_057107.4:p.Gln31His
XM_011517129.2:c.-347G>C	XP_011515431.2:n.-347G>C
NM_016023.5:c.93G>C MANE Select	NP_057107.4:p.Gln31His
NM_001286745.3:c.-351G>C	NP_001273674.1:n.-351G>C